NDC 68220-160 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68220-160 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA019715 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1990-07-31 |
| Marketing End Date | 2017-05-11 |